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氧化生物电催化:从天然代谢途径到合成代谢体和最小酶级联反应。

Oxidative bioelectrocatalysis: From natural metabolic pathways to synthetic metabolons and minimal enzyme cascades.

作者信息

Minteer Shelley D

机构信息

Departments of Chemistry and Materials Science & Engineering, University of Utah, 315 S 1400 E Rm 2020, Salt Lake City, UT 84112, USA.

出版信息

Biochim Biophys Acta. 2016 May;1857(5):621-624. doi: 10.1016/j.bbabio.2015.08.008. Epub 2015 Sep 1.

Abstract

Anodic bioelectrodes for biofuel cells are more complex than cathodic bioelectrodes for biofuel cells, because laccase and bilirubin oxidase can individually catalyze four electron reduction of oxygen to water, whereas most anodic enzymes only do a single two electron oxidation of a complex fuel (i.e. glucose oxidase oxidizing glucose to gluconolactone while generating 2 electrons of the total 24 electrons), so enzyme cascades are typically needed for complete oxidation of the fuel. This review article will discuss the lessons learned from natural metabolic pathways about multi-step oxidation and how those lessons have been applied to minimal or artificial enzyme cascades. This article is part of a Special Issue entitled Biodesign for Bioenergetics--the design and engineering of electronic transfer cofactors, proteins and protein networks, edited by Ronald L. Koder and J.L. Ross Anderson.

摘要

用于生物燃料电池的阳极生物电极比阴极生物电极更为复杂,因为漆酶和胆红素氧化酶能够各自催化氧气的四电子还原生成水,而大多数阳极酶仅对复杂燃料进行单个的双电子氧化反应(例如葡萄糖氧化酶将葡萄糖氧化为葡萄糖酸内酯,同时在总共24个电子中产生2个电子),所以通常需要酶级联反应来实现燃料的完全氧化。这篇综述文章将讨论从天然代谢途径中汲取的关于多步氧化的经验教训,以及这些经验教训是如何应用于最小化或人工酶级联反应的。本文是名为《生物能量学的生物设计——电子转移辅因子、蛋白质和蛋白质网络的设计与工程》特刊的一部分,该特刊由罗纳德·L·科德和J.L.罗斯·安德森编辑。

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